CN109154047A - Method for manufacturing the steel plate through replying with austenitic matrix - Google Patents
Method for manufacturing the steel plate through replying with austenitic matrix Download PDFInfo
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- CN109154047A CN109154047A CN201780030117.6A CN201780030117A CN109154047A CN 109154047 A CN109154047 A CN 109154047A CN 201780030117 A CN201780030117 A CN 201780030117A CN 109154047 A CN109154047 A CN 109154047A
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Abstract
The present invention relates to a kind of methods for producing the steel plate through replying with austenitic matrix with expected mechanical property.
Description
The present invention relates to a kind of methods for producing the steel plate through replying with austenitic matrix.The present invention is particularly
Suitable for manufacturing motor vehicles.
In order to save the weight of vehicle, it is known to use high strength steel is for manufacturing motor vehicles.For example, for structure member
Manufacture, it is necessary to improve the mechanical property of such steel.However, although the intensity of steel is improved, the extension of high-carbon steel
Rate reduces, and therefore formability can also reduce.In order to overcome these problems, the steel plate through replying is had already appeared, especially
It is the twin crystal induction plastic steel (TWIP steel) with good formability.Although product shows extraordinary formability,
Mechanical property such as ultimate tensile stress and yield stress may be not high enough and be unable to satisfy automobile application.
In order to improve the intensity of these steel while keeping good machinability, it is known that induced by cold rolling highly dense
Then the twin of degree removes dislocation by reply processing but retains twin.
However, there is the risk that cannot obtain expected mechanical property by applying such method.In fact, ability
The technical staff in domain can only in accordance with known methods, and whether then measure realizes the phase from the point of view of the mechanical property of steel plate obtained
The mechanical property of prestige.Can not the condition of method of adjustment obtain expected mechanical property.
Therefore, the purpose of the present invention is to a kind of show at least one expected mechanical property for manufacturing by providing
The method of steel plate through replying solves disadvantages mentioned above, and such mechanical property improved.Another purpose is to provide one kind
The steel plate through replying with the mechanical property improved in this way.
The purpose is realized by providing the method according to claim 1 for being used to manufacture TWIP steel plate.This method
It can also include the feature of claim 2 to 20.
Another purpose is realized by providing TWIP steel plate according to claim 21.
Other features and advantages of the present invention will be by of the invention described in detail below and become obvious.
Following term will be defined:
- M: mechanical property
-MTarget: the target value of mechanical property,
-MRecrystallization: the mechanical property after recrystallization annealing,
-MCold rolling: the mechanical property after cold rolling,
- UTS: ultimate tensile strength,
- TE: breaking elongation,
- P:pareq value,
-PTarget: the target value of pareq,
The full width at half maximum (FWHM) of-FWHM:X Ray Diffraction Spectroscopy, and
-FWHMTarget: the target value of the full width at half maximum (FWHM) of X-ray diffraction spectra.
The present invention relates to a kind of method for manufacturing the steel plate through replying with austenitic matrix, the steel plate performance
It is equal to or more than target value M outTargetAt least one mechanical property (M), the composition of the steel plate includes by weight:
0.1% < C < 1.2%,
13.0%≤Mn < 25.0%,
S≤0.030%,
P≤0.080%,
N≤0.1%,
Si≤3.0%,
And on the basis of entirely optional, one or more of elements such as below,
Nb≤0.5%,
B≤0.005%,
Cr≤1.0%,
Mo≤0.40%,
Ni≤1.0%,
Cu≤5.0%,
Ti≤0.5%,
V≤2.5%,
Al≤4.0%,
The remainder of composition is constituted by iron and by the inevitable impurity that exploitation generates,
This method includes being step below:
A. calibration steps, in which:
I. prepare have been subjected to 400 DEG C to 900 DEG C the heat treatment during 40 seconds to 60 minutes described steel at least two
Sample, the heat treatment correspond to Pareq value P,
II. X-ray diffraction is carried out to obtain the spectrum including main peak to the sample, measures the main peak in half eminence
Width FWHM,
III. the M of such sample is measured,
IV. the reply or recrystallization state of each sample are measured,
V. song of the M as the function of FWMH is drawn in the region that wherein sample is returned to 100% but does not recrystallize from 0
Line,
B. step is calculated, in which:
I. it determines and corresponds to MTargetFWHMTargetValue,
II. it determines and carries out to reach such MTargetHeat treatment pareq value PTarget, and
III. selection corresponds to PTargetThe time t of valueTargetWith T ° of temperatureTarget,
C. there is MRecrystallizationRecrystallization steel plate offer step,
D. in order to obtain with MCold rollingSteel plate cold rolling step, and
E. at T ° of temperatureTargetUnder in time tTargetThe annealing steps that period carries out.
It is not intended to by any theoretical constraint, it appears that when applying the method according to the invention, annealing steps can be obtained
E technological parameter) has the steel plate through replying of expected improved mechanical property, especially TWIP steel plate to obtain.
About the chemical composition of steel, C plays an important role in terms of the formation of microscopic structure and mechanical property.Which increase
Stacking fault energy and the stability for promoting austenite phase.It is mixed when with the Mn of content by weight 13.0% to 25%
When, carbon content obtains this stability when being 0.5% or higher.There are vanadium carbide, high Mn content can increase
Add solubility of the vanadium carbide (VC) in austenite.However, having the C content for being greater than 1.2% due to such as vanadium carbide
Or the excess of carboritride is precipitated and causes the risk of ductility reduction.Preferably, carbon content by weight 0.4% to
1.2%, more preferably 0.5% to 1.0% to obtain enough intensity.
Mn is also for improving intensity, for increasing stacking fault energy and for the essential elements of stable austenite phase.Such as
Then there is the risk for forming martensitic phase, this is readily apparent that reduce deformability less than 13.0% in its content of fruit.In addition,
When manganese content is greater than 25.0%, the formation of twin is suppressed, and therefore, although intensity increases, ductility at room temperature is reduced.It is excellent
Selection of land, manganese content are 15.0% to 24.0%, and more preferably 17.0% to 24.0% to optimize stacking fault energy and prevent
Martensite is formed under anamorphic effect.In addition, when Mn content is greater than 24.0%, by the deformation pattern of twin not over complete
The deformation pattern of perfect dislocation sliding is advantageous.
Al is the particularly effective element of deoxidation to steel.As C, which increase stacking fault energies, and it reduce formation
The risk of martensite is deformed, so as to improve ductility and anti-delayed fracture resistance.However, if Al is in the steel with high Mn content
It is present in excess, then Al is a disadvantage, because Mn improves solubility of the nitrogen in molten iron.If existed in steel a large amount of
Al, the then N combined with Al are precipitated in the form of aln precipitation (AlN), this hindered during thermal transition the migration of crystal boundary and
It is readily apparent that increase cracked risk in continuous casting.In addition, as described below, it is necessary to which there have the N of sufficient amount to be thin to be formed
Precipitate, substantially carbonitride.Preferably, Al content is less than or equal to 2%.When Al content is greater than 4.0%, there is suppression
Make the risk for forming twin and reducing ductility.Preferably, the amount of Al is greater than 0.06% and more preferably larger than 0.7%.
Correspondingly, nitrogen content is necessary for 0.1% or smaller to prevent precipitation and the volume defect (gas of AlN during solidification
Bubble) formation.In addition, when in the presence of can be with element (such as vanadium, niobium, titanium, chromium, molybdenum and boron) of nitride form precipitation, nitrogen
Content must not exceed 0.1%.
According to the present invention, the amount of V is less than or equal to 2.5%, it is therefore preferable to 0.1% to 1.0%.Preferably, V-arrangement is at precipitation
Object.Preferably, volume fraction of such element in steel is 0.0001% to 0.025%.Preferably, the most numerical digit of vanadium
In the position in crystal grain.Advantageously, the average-size of vanadium is less than 7nm, it is therefore preferable to 1nm to 5nm and more preferably
0.2nm to 4.0nm.
Silicon is also for making steel-deoxidizing and for the effective element of solid phase hardening.However, being greater than 3% content, silicon is reduced
Elongation percentage and during certain assembling process tend to form undesirable oxide, it is therefore necessary to it be made to remain less than the limit
System.Preferably, the content of silicon is less than or equal to 0.6%.
Sulphur and phosphorus are the impurity for making embrittlement of grain boundaries.Their own content must not exceed 0.030% and 0.080% to protect
Hold enough hot ductilitys.
Some boron can be added, are up to 0.005%, preferably up to 0.001%.The element is segregated simultaneously in grain boundaries
And increase their cohesive force.It is not wishing to be bound by theory, it is believed that this causes to subtract by residual stress after compression moulding
It is small and preferably anticorrosive under the stress of the component thus shaped.The element is segregated and is increased at austenite grain boundary
Their cohesive force.Boron is precipitated for example in the form of boron-carbide and boron nitride.
Nickel can be optionally for the intensity for improving steel by solution hardening.However, for cost reasons etc., it is desirable to it will
Nickel content is limited to maximum level and is 1.0% or smaller and is preferably lower than 0.3%.
Similarly, optionally, copper of the addition content no more than 5% is a kind of side by the precipitation-hardening steel of copper metal
Formula.However, being greater than the content, copper is the reason of causing the surface defect of the plate of hot rolling to occur.Preferably, the amount of copper is less than
2.0%.Preferably, the amount of Cu is greater than 0.1%.
Titanium and niobium are also can be optionally for the element realizing hardening by forming precipitate and strengthening.However, working as Nb
Or Ti content be greater than 0.50% when, exist excessively be precipitated may cause toughness reduction risk, this must be avoided.Preferably, Ti
Amount by weight 0.040% to 0.50% or by weight 0.030% to 0.130%.Preferably, Ti content is by weight
It is calculated as 0.060% to 0.40% and such as 0.060% to 0.110%.Preferably, the amount of Nb is greater than 0.01% simultaneously by weight
And more preferably 0.070% to 0.50% or 0.040% to 0.220%.Preferably, content of niobium is by weight
0.090% to 0.40% and it is advantageously 0.090% to 0.200%.
Chromium and molybdenum may be used as the optional elements of the intensity for improving steel by solution hardening.However, since chromium reduces
Stacking fault energy, so its content must not exceed 1.0% and preferably 0.070% to 0.6%.Preferably, chromium contains
Amount is 0.20% to 0.5%.Molybdenum can be with 0.40% or smaller amount, preferably 0.14% to 0.40% amount addition.
Furthermore, it is undesirable to theoretical be constrained by any, it appears that vanadium, titanium, niobium, chromium and molybdenum precipitate can reduce lag and open
The sensibility split, and do so and will not reduce ductility and property of toughness.It is therefore preferred that selected from carbide, nitride and
At least one of titanium, niobium, chromium and the molybdenum of carbonitride form element is present in steel.
According to the present invention, the method includes calibration steps A.I), wherein prepare have been subjected to 400 DEG C to 900 DEG C
At least two sample of heat-treated steel plate during 40 seconds to 60 minutes, the sample, the heat treatment correspond to Pareq value P.
In this step, determine the parameter for being known as Pareq the different heat treatment of different time can be carried out more at different temperatures,
It passes through defined below:
Pareq=-0.67*log(∫-ΔH/RT)*dt)
Wherein Δ H: diffusion energy (be equal to 300kJ/mol) of the iron in iron, the temperature of T=circulation integrate as in entire heat
It handles on the time.Heat treatment is hotter or more long, and Pareq value is lower.Two different heat treatments with identical Pareq value will be
Identical result is provided on identical steel grade.Preferably, Pareq value is greater than 14.2, more preferably 14.2 to 25 and more preferably
14.2 to 18.
Then during the step A.II), X-ray diffraction is carried out to sample to obtain the spectrum including main peak, described in measurement
The full width at half maximum (FWHM) FWHM of main peak.X-ray diffraction is a kind of non-destructive analysis technology, is provided brilliant about the inside of crystalline material
The details of lattice, the details including unit cell dimension, bond distance, bond angle and site sequence (site-ordering).Directly related
It is monocrystalline refine, wherein the data generated by X-ray analysis are explained and refine is to obtain crystal structure.In general, X-ray crystal
Be the tool of such crystal structure for identification.According to the present invention, steel plate has austenitic matrix, and austenitic matrix has
Face-centered cubic system.It is therefore preferred that the main peak of measurement full width at half maximum (FWHM) FWHM corresponds to Miller indices [311].In fact, recognizing
It is the best representative that dislocation density influences for the peak (for the feature of austenite system).
Then, during step A.III), the M of such sample is measured.Preferably, M be ultimate tensile strength (UTS),
Breaking elongation (TE) or both (UTS*TE).
After the reply or recrystallization state that measure each sample during step A.IV).Preferably, aobvious with scanning electron
Micro mirror (SEM) and EBSD (electron backscatter diffraction) or transmission electron microscope (TEM) measure such state.
Then, during step A.V), M is drawn in the region that wherein sample is returned to 100% but does not recrystallize from 0
The curve of function as FWMH.
According to the present invention, it realizes and calculates step B).Calculating includes step B.I), correspond to M wherein determiningTargetFWHMTarget
Value.Preferably, FWHMTargetGreater than 1.0 ° and it is advantageously 1.0 ° to 1.5 °.
In a preferred embodiment, wherein M is UTS, and the determination of FWHM is realized using following formula:
UTSTarget=UTSCold rolling-(UTSCold rolling-UTSRecrystallization)*(exp((-FWHM+2.3)/2.3)-1)4)
In that case it is preferable that UTSTargetMore than or equal to 1430MPa and more preferably 1430MPa extremely
2000MPa。
In another preferred embodiment, wherein M is TE, utilize following formula realize calculate step B.I) during FWHM
Determination:
TETarget=TECold rolling-(TERecrystallization-UTSCold rolling)*(exp((-FWHM+2.3)/2.3)-1)2.5)
In that case it is preferable that TETargetMore than or equal to 15% and more preferably 15% to 30%.
In another preferred embodiment, wherein M is UTS*TE, is realized using following formula and calculates step B.I) during
The determination of FWHM:
UTSTarget *TETarget=100000*(1-0.5FWHM)
In that case it is preferable that UTSTarget*TETargetGreater than 21000 and more preferably 21000 to 60000,
TETargetIt is up to 30%.
Then, step B.II is carried out), it carries out wherein determining to reach such MTargetHeat treatment pareq value PTarget。
Preferably, PTargetGreater than 14.2, more preferably 14.2 to 25 and more preferably 14.2 to 18.
Later, it is realised in that selection corresponds to PTargetThe time t of valueTargetWith T ° of temperatureTargetStep B.III).Preferably,
T°TargetIt is 400 DEG C to 900 DEG C, tTargetIt is 40 seconds to 60 minutes.
It then, according to the method for the present invention include that there is MRecrystallizationRecrystallization steel plate offer step.In fact it is preferred to
Ground, 700 DEG C to 900 DEG C at a temperature of the recrystallization annealing that carries out after steel plate recrystallize.For example, recrystallizing at 10 seconds extremely
It is realized during 500 seconds, preferably 60 seconds to 180 seconds.
In a preferred embodiment, when M is UTS, UTSRecrystallizationGreater than 800MPa, it is therefore preferable to which 800MPa is extremely
1400MPa and more preferably 1000MPa are to 1400MPa.
In another preferred embodiment, when M is TE, TERecrystallizationGreater than 20%, preferably more than 30% and more
Preferably 30% to 70%.
In another preferred embodiment, when M is TE*UTS, TERecrystallization*UTSRecrystallizationGreater than 16000, more preferably
Greater than 24000 and it is advantageously 24000 to 98000.
Then, cold rolling step D is realized) there is M to obtainCold rollingSteel plate.Preferably, reduction ratio is 1% to 50%, preferably
Ground 1% to 25% or 26% to 50%.It allows steel thickness to reduce.In addition, can be through according to the steel plate of above method manufacture
By by undergoing the strain hardening of the milling step that there is the intensity improved.In addition, the step induces highdensity twin, from
And improve the mechanical property of steel plate.
In a preferred embodiment, when M is UTS, UTSCold rollingGreater than 1000, preferably more than 1200MPa and
Be advantageously greater than 1400MPa.
In another preferred embodiment, when M is TE, TECold rollingGreater than 2%, more preferably 2% to 50%.
In another preferred embodiment, when M is TE*UTS, TECold rolling*UTSCold rollingGreater than 2000, preferably 2400
And more preferably 2400 to 70000.
Then, in time tTargetPeriod is at T ° of temperatureTargetIt is lower to carry out annealing steps E).
After the second cold rolling, hot dip coating step G can be carried out).Preferably, step G) using based on aluminium bath or be based on
The bath of zinc is realized.
In a preferred embodiment, hot-dip step is carried out using the bath based on aluminium comprising following component: small
Si in 15%, the Fe less than 5.0%, optionally 0.1% to 8.0% Mg and optionally 0.1% to 30.0% Zn, it is remaining
Part is Al.
In another preferred embodiment, hot-dip step is carried out with the bath based on zinc comprising following component:
0.01% to 8.0% Al, optionally 0.2% to 8.0% Mg, remainder Zn.
Liquid-bath can also be comprising from providing ingot or the inevitable impurity passed through from steel plate in liquid-bath and residual
Remaining element.For example, optional impurity is selected from Sr, Sb, Pb, Ti, Ca, Mn, Sn, La, Ce, Cr, Zr or Bi, every kind of other element
Content by weight be lower than 0.3 weight %.The residual elements passed through from offer ingot or from steel plate in liquid-bath can
Think that content is up to 5.0 weight %, the preferably iron of 3.0 weight %.
For example, annealing steps can be carried out after coating deposition to obtain the steel plate through zinc-plated diffusion annealing.
Therefore, the tool at least one expection and improved mechanical property is obtained by application according to the method for the present invention
There is the steel plate through replying of austenitic matrix.
Embodiment
In this embodiment, using the steel plate formed with following weight:
C (%) | Mn (%) | Si (%) | P (%) | Al (%) | Cu (%) | Mo (%) | V (%) | N (%) | Nb (%) | Cr (%) | Ni (%) |
0.583 | 21.9 | 0.226 | 0.03 | 0 | 0.031 | 0.01 | 0.206 | 0.0148 | 0 | 0.183 | 0.06 |
In this embodiment, the target value M of the mechanical property of the steel plate through replyingTargetFor the UTS of 1512MPaTarget.Due to school
Quasi- step A is determined and is corresponded to UTSTargetFWHMTargetValue, FWHMTargetIt is 1.096.It determines and carries out to reach UTSTargetHeat at
The P of reasonTarget, it is 14.39.Then, the time t of selectionTargetFor 40 seconds and select T ° of temperatureTargetIt is 650 DEG C.
Therefore, firstly, by test 1 and 2 1200 DEG C at a temperature of heating and hot rolling.The finishing temperature of hot rolling is set as
It 890 DEG C and is batched at 400 DEG C after hot rolling.Then, the first cold rolling is realized with 50% cold rolling reduction ratio.This
Afterwards, recrystallization annealing is carried out at 825 DEG C during 180 seconds.UTS obtainedRecrystallizationValue be 980MPa.Then, second is cold
It rolls and is realized with 30% cold rolling reduction ratio.UTS obtainedCold rollingValue be 1540MPa.
Then, it anneals at 650 DEG C to test 1 during 40 seconds according to the present invention.After the annealing, to test
1 is replied.The UTS of test 1 is 1512.5MPa.
It anneals, i.e., does not consider through determination according to the method for the present invention to test 2 at 650 DEG C during 90 seconds
tTargetWith T °Target.After the annealing, test 2 is recrystallized.The UTS of test 2 is 1415.15MPa.The FMHM of trial target 2 is
0.989 and P is 14.12, i.e., except the scope of the present invention.
The result shows that when applying the method according to the invention, being replied with expected mechanical property can be obtained
Steel plate.
Claims (21)
1. a kind of method for manufacturing the steel plate through replying with austenitic matrix, the steel plate show to be equal to or more than
Target value MTargetAt least one mechanical property (M), the composition of the steel plate includes by weight:
0.1% < C < 1.2%,
13.0%≤Mn < 25.0%,
S≤0.030%,
P≤0.080%,
N≤0.1%,
Si≤3.0%,
And on the basis of entirely optional, one or more of elements such as below
Nb≤0.5%,
B≤0.005%,
Cr≤1.0%,
Mo≤0.40%,
Ni≤1.0%,
Cu≤5.0%,
Ti≤0.5%,
V≤2.5%,
Al≤4.0%,
The remainder of the composition is constituted by iron and by the inevitable impurity that exploitation generates,
Such method includes being step below:
A. calibration steps, in which:
I. prepare have been subjected to 400 DEG C to 900 DEG C the heat treatment during 40 seconds to 60 minutes the steel at least two sample
Product, the heat treatment correspond to Pareq value P,
II. X-ray diffraction is carried out to obtain the spectrum including main peak to the sample, measures the main peak in width at half height
FWHM,
III. the M of such sample is measured,
IV. the reply or recrystallization state of each sample are measured,
V. song of the M as the function of FWMH is drawn in the region that the wherein sample is returned to 100% but does not recrystallize from 0
Line,
B. step is calculated, in which:
I. it determines and corresponds to the MTargetFWHMTargetValue,
II. it determines and carries out to reach such MTargetThe heat treatment the pareq value PTarget, and
III. selection corresponds to the PTargetThe time t of valueTargetWith T ° of temperatureTarget,
C. there is MRecrystallizationRecrystallization steel plate offer step,
D. in order to obtain with MCold rollingSteel plate cold rolling step, and
E. at T ° of temperatureTargetUnder in time tTargetThe annealing steps that period carries out.
2. according to the method described in claim 1, wherein the steel plate occurs after 700 DEG C to 900 DEG C realization recrystallization annealing
Recrystallization.
3. method according to claim 1 or 2, wherein the cold rolling is realized with 1% to 50% reduction ratio.
4. according to the method in any one of claims 1 to 3, wherein in the calibration steps A.II) during, half eminence
The measured main peak of width FWHM correspond to Miller indices [311].
5. method according to claim 1 to 4, wherein M is ultimate tensile strength (UTS), breaking elongation
(TE) or both (UTS*TE).
6. according to the method described in claim 5, realized using following formula wherein when M is UTS and calculate step B.I) during
The determination of FWHM:
UTSTarget=UTSCold bundle-(UTSCold rolling-UTSRecrystallization) * (exp ((- FWHM+2.3)/2.3) -1)4)。
7. method according to claim 5 or 6, wherein when the M is UTS, the UTSTargetIt is greater than or equal to
1430MPa。
8. according to the method described in claim 7, the wherein UTSTargetFor 1430MPa to 2000MPa.
9. according to the method described in claim 5, realized using following formula wherein when M is TE and calculate step B.I) during
The determination of FWHM:
TETarget=TECold bundle-(TERecrystallization-UTSCold bundle) * (exp ((- FWHM+2.3)/2.3) -1)2.5)。
10. the method according to any one of claim 5 or 9, wherein when M is TE, TETargetMore than or equal to 15%.
11. according to the method described in claim 10, wherein TETargetIt is 15% to 30%.
12. according to the method described in claim 5, realized using following formula wherein when M is TE*UTS and calculate step B.I) during
FWHM determination:
UTSTarget* TETarget=100000* (1-0.5FWHM).
13. method according to any one of claim 1 to 12, wherein when M is TE*UTS, UTSTarget*TETargetIt is greater than
21000, TETargetIt is up to 30%.
14. according to the method for claim 13, wherein UTSTarget*TETargetIt is 21000 to 60000, TETargetIt is up to 30%.
15. according to claim 1 to method described in any one of 14, wherein FWHMTargetMore than or equal to 1.0 °.
16. according to the method for claim 15, wherein FWHMTargetIt is 1.0 ° to 1.5 °.
17. according to claim 1 to method described in any one of 16, wherein PTargetGreater than 14.2.
18. according to the method for claim 17, wherein PTargetIt is 14.2 to 25.
19. according to the method for claim 18, wherein PTargetIt is 14.2 to 18.
20. according to the method for claim 19, wherein T °TargetIt is 400 DEG C to 900 DEG C, tTargetIt is 40 seconds to 60 minutes.
21. one kind can be as according to claim 1 to the warp with austenitic matrix that method described in any one of 20 obtains
The TWIP steel plate of reply.
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PCT/IB2016/000698 WO2017203313A1 (en) | 2016-05-24 | 2016-05-24 | Method for the manufacture of a recovered steel sheet having an austenitic matrix |
PCT/IB2017/000628 WO2017203350A1 (en) | 2016-05-24 | 2017-05-23 | Method for the manufacture of a recovered steel sheet having an austenitic matrix |
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WO2020115526A1 (en) | 2018-12-04 | 2020-06-11 | Arcelormittal | Cold rolled and annealed steel sheet, method of production thereof and use of such steel to produce vehicle parts |
WO2020128591A1 (en) * | 2018-12-20 | 2020-06-25 | Arcelormittal | Method for the manufacture of a recovered steel sheet having an austenitic matrix |
EP4455349A1 (en) * | 2021-12-21 | 2024-10-30 | POSCO Co., Ltd | Austenitic steel having excellent ultra-low temperature toughness in weld heat-affected zone, and manufacturing method therefor |
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